EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS180-03112 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:153492270-153493870 
TF binding sites/motifs
Number: 26             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:153492670-153492688GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr1:153492674-153492692GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr1:153492692-153492710GGAGGGAGGGAGGGAGGG+6.03
IRF1MA0050.2chr1:153492767-153492788AGAGAGAAAAAGAAAGAAAGA-6.22
KLF16MA0741.1chr1:153492989-153493000GGGGGCGGGGC-6.02
KLF5MA0599.1chr1:153492990-153493000GGGGCGGGGC-6.02
PBX1MA0070.1chr1:153492921-153492933ACATCAATCAAT+6.44
SP1MA0079.4chr1:153492988-153493003AGGGGGCGGGGCTTC-6.79
SP2MA0516.2chr1:153492987-153493004AAGGGGGCGGGGCTTCC-7.44
SP4MA0685.1chr1:153492986-153493003GAAGGGGGCGGGGCTTC-7.66
ZNF263MA0528.1chr1:153492663-153492684GAGAGAGGGAGGGAGGGAGGG+6.11
ZNF263MA0528.1chr1:153492717-153492738GAGAGAGGGAGGGAGGGAGGG+6.11
ZNF263MA0528.1chr1:153492707-153492728GGGGGAGAGAGAGAGAGGGAG+6.13
ZNF263MA0528.1chr1:153492647-153492668AGAGGAGAGAGAGAGAGAGAG+6.22
ZNF263MA0528.1chr1:153492729-153492750GAGGGAGGGAGAGAGAGAGAG+6.89
ZNF263MA0528.1chr1:153492725-153492746GAGGGAGGGAGGGAGAGAGAG+6.9
ZNF263MA0528.1chr1:153492701-153492722GAGGGAGGGGGAGAGAGAGAG+7.06
ZNF263MA0528.1chr1:153492679-153492700GAGGGAGGGAGGGGGAGGGAG+7.15
ZNF263MA0528.1chr1:153492675-153492696GAGGGAGGGAGGGAGGGGGAG+7.23
ZNF263MA0528.1chr1:153492693-153492714GAGGGAGGGAGGGAGGGGGAG+7.23
ZNF263MA0528.1chr1:153492683-153492704GAGGGAGGGGGAGGGAGGGAG+7.32
ZNF263MA0528.1chr1:153492697-153492718GAGGGAGGGAGGGGGAGAGAG+7.35
ZNF263MA0528.1chr1:153492721-153492742GAGGGAGGGAGGGAGGGAGAG+7.43
ZNF263MA0528.1chr1:153492667-153492688GAGGGAGGGAGGGAGGGAGGG+7.97
ZNF263MA0528.1chr1:153492671-153492692GAGGGAGGGAGGGAGGGAGGG+7.97
ZNF263MA0528.1chr1:153492689-153492710GGGGGAGGGAGGGAGGGAGGG+8.55
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_23261chr1:153492648-153493055Colon_Crypt_1
SE_23261chr1:153493085-153493774Colon_Crypt_1
SE_23926chr1:153492684-153493009Colon_Crypt_2
SE_23926chr1:153493191-153493642Colon_Crypt_2
SE_25303chr1:153492612-153493815Colon_Crypt_3
SE_28418chr1:153492480-153494160Fetal_Intestine
SE_52579chr1:153492604-153493885Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1153493081153493571
chr1153493395153493807
Number: 1             
IDChromosomeStartEnd
GH01I153520chr1153492710153493995
Enhancer Sequence
TTAAAGCACC AAAAACCTTG TATTAGTTTT TTAAATAAAT TTTTGGAAGT GTGAACCTCC 60
AAAATTTGAG ACAGGTCTCA ATTAATTTAG AAAGTTTATT CTGCCAGTGC CAGGCGCGGT 120
GGCTCAAGCC TGTAATCCCA GCACTTTGGG AGGCTCAGGG GGGCGGAACA CGAGGTCAGC 180
AGTTTGAGAC CAGCCTGACC AACATGGTGA AACCCTGTCT CTACTAAAAA TACAAAAATT 240
AGCTAGGCGT GGTGGCACGC ACCTGTAATC CCAGCTACTG GGGAAGCTGA GACAGGAGAA 300
TTGCTTGAAC CCGGGAGGCA GAGGTTGCAG TGAGCTGAGA TCGTGCCACG GCACTCCAGC 360
CTGAAAAAGA GAAAGAAAGA GGAGAGAGAG AGAGAGAGAG GGAGGGAGGG AGGGAGGGAG 420
GGGGAGGGAG GGAGGGAGGG GGAGAGAGAG AGAGGGAGGG AGGGAGGGAG AGAGAGAGAG 480
AGAGAGAAGA GAGAGAGAGA GAGAAAAAGA AAGAAAGAAA GTTTATTTTG CCAAGATTGA 540
GGACACAGCC TCAGGAGGCA CCCGTGACAC AGCCTCATGA CAGGTCCTGA TGACATGTGC 600
CCAAGGTGGT CAGGGCACAG CTTGGTTTTA AACATTTTAG GGAGACATGC GACATCAATC 660
AATATATTTA AAATGAACAT TGGTTAGGTC CGGAAAGGTG GGACAGCTTG AAGCAAGAAG 720
GGGGCGGGGC TTCCAGGTCA CAGGTAGATG AGAGACAAAG GTTGCATTCT TTTGAGTTTC 780
TGATTAGCCT CTCCAAAGGA GGCAATCAGA TATGCATTTA TCTCAGTGAG CAGAGGGGTG 840
ACTTTGAGTA GAATGGGAGG CAGGTTTGCC CTGAGCAGTT CCTAGCTTGA TTCTTCCTTT 900
TAGCTTAGTG ATCTGGGTCC AAGATATATT CCTCTCACTG AAAAAACCAC ACATATAATA 960
GTTAAAGTGA GTGTCCAAGC CAAAAGAGTC TAGGAAGAGG CCCCAGAGCC CTGGCCATAG 1020
GCATGCCCCT TACTCTGTTA GCTAAATAAC ATCCCTGGGC CTGTTAAATC TACATGCTGC 1080
CTTTGTACAA ATGAGAAAAA GGTGTCTCAT CCTCTAGGCA GAGGTAGCCA GGCACCGAGG 1140
TGGTGGCTTA GAAAGCTCAG CACAGGCTGA ATTTCAGCCC TCACTGATTC CCCTAGCATG 1200
AGCTTTTTGT GCAGGACACA GATTGGAGGG CTGTTCTCAG CAGCTCTGCC TAGGGTAACT 1260
CCAGGGAGCA CAGCCTTAAC ACTATAGACT AGACCGTCTC TAACATCCCA CCCAGCTCTG 1320
GTTTATCAGA CTTCTTCAAT TCCATAGCCT CACTCCTGAA CAAAGCAGTT GGGCTATGTA 1380
TTTTTGTGAG ATACCTATCG CAGCTATTAA ATCCATTAAA ACCAAGTATC TTAAGTAAAC 1440
TGAAATGACT TCTGAATTGC TGTGGTCAGG CAGTTCCCTC AGGGCGAAGC ATGGATCTCA 1500
ACCATCAGGG CAGCCCCAGC AATAAGGATG GCTCCTGCCA CACAGAAGGC ACACTCTGAG 1560
TACACATGTA TTGAATAAAA CAATAAATAA TGACAGGATA 1600